Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: E9ATX9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0032182 | ubiquitin-like protein binding | 3 | 1 |
GO:0043130 | ubiquitin binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.692 |
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.576 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.758 |
CLV_PCSK_FUR_1 | 54 | 58 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.760 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.720 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.613 |
DEG_APCC_DBOX_1 | 45 | 53 | PF00400 | 0.614 |
DOC_AGCK_PIF_2 | 355 | 360 | PF00069 | 0.517 |
DOC_CKS1_1 | 206 | 211 | PF01111 | 0.733 |
DOC_CYCLIN_RxL_1 | 43 | 51 | PF00134 | 0.638 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 523 | 532 | PF00134 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 29 | 35 | PF00134 | 0.685 |
DOC_MAPK_gen_1 | 315 | 324 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 315 | 324 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 596 | 604 | PF00069 | 0.528 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.802 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.704 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.801 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.559 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.724 |
LIG_14-3-3_CanoR_1 | 277 | 282 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 294 | 302 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 587 | 593 | PF00244 | 0.492 |
LIG_APCC_ABBA_1 | 153 | 158 | PF00400 | 0.480 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.518 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.669 |
LIG_BRCT_BRCA1_1 | 520 | 524 | PF00533 | 0.677 |
LIG_deltaCOP1_diTrp_1 | 581 | 589 | PF00928 | 0.572 |
LIG_eIF4E_1 | 156 | 162 | PF01652 | 0.611 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.510 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.766 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.522 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.431 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.427 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.584 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.605 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.623 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.720 |
LIG_Integrin_isoDGR_2 | 3 | 5 | PF01839 | 0.808 |
LIG_LIR_Gen_1 | 588 | 594 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 564 | 568 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.522 |
LIG_Pex14_1 | 302 | 306 | PF04695 | 0.527 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.739 |
LIG_Rb_pABgroove_1 | 150 | 158 | PF01858 | 0.584 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.595 |
LIG_SH2_CRK | 436 | 440 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.641 |
LIG_SH3_2 | 206 | 211 | PF14604 | 0.793 |
LIG_SH3_2 | 415 | 420 | PF14604 | 0.700 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.769 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.778 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.476 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.729 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.771 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.764 |
LIG_SUMO_SIM_par_1 | 149 | 158 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.717 |
LIG_SUMO_SIM_par_1 | 368 | 374 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 458 | 464 | PF11976 | 0.552 |
LIG_TYR_ITIM | 434 | 439 | PF00017 | 0.663 |
LIG_UBA3_1 | 532 | 540 | PF00899 | 0.559 |
LIG_UBA3_1 | 600 | 606 | PF00899 | 0.505 |
LIG_WRPW_2 | 336 | 339 | PF00400 | 0.476 |
MOD_CDK_SPxK_1 | 205 | 211 | PF00069 | 0.677 |
MOD_CDK_SPxK_1 | 434 | 440 | PF00069 | 0.409 |
MOD_CDK_SPxxK_3 | 183 | 190 | PF00069 | 0.719 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.685 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.684 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.564 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.720 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.661 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.774 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.721 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.608 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.597 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.688 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.474 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.436 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.733 |
MOD_Cter_Amidation | 3 | 6 | PF01082 | 0.724 |
MOD_Cter_Amidation | 407 | 410 | PF01082 | 0.750 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.811 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.664 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.709 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.752 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.692 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.652 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.676 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.369 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.391 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.652 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.618 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.569 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.614 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.784 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.683 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.608 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.664 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.692 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.534 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.670 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.440 |
MOD_NEK2_2 | 151 | 156 | PF00069 | 0.584 |
MOD_NEK2_2 | 485 | 490 | PF00069 | 0.583 |
MOD_NEK2_2 | 519 | 524 | PF00069 | 0.588 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.604 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.786 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.691 |
MOD_PK_1 | 277 | 283 | PF00069 | 0.590 |
MOD_PKA_1 | 6 | 12 | PF00069 | 0.709 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.804 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.680 |
MOD_PKB_1 | 88 | 96 | PF00069 | 0.659 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.432 |
MOD_Plk_2-3 | 75 | 81 | PF00069 | 0.729 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.541 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.643 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.416 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.734 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.679 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.656 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.644 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.699 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.607 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.727 |
MOD_SUMO_for_1 | 578 | 581 | PF00179 | 0.623 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.687 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.599 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.589 |
TRG_ER_diArg_1 | 409 | 411 | PF00400 | 0.762 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.796 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.676 |
TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMT0 | Leptomonas seymouri | 55% | 97% |
A0A0S4JTW8 | Bodo saltans | 34% | 100% |
A0A1X0P060 | Trypanosomatidae | 34% | 100% |
A0A3R7LYT2 | Trypanosoma rangeli | 32% | 100% |
A0A3S7XBW1 | Leishmania donovani | 90% | 99% |
A4HQ59 | Leishmania braziliensis | 76% | 100% |
A4IDV8 | Leishmania infantum | 90% | 99% |
D0A458 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4Q0L7 | Leishmania major | 92% | 100% |
V5BQB1 | Trypanosoma cruzi | 34% | 100% |